(R,S)-2-Amino-3-(5-hydroxy-2-propyl-2H-1,2,3-triazol-4-yl)propanoic Acid

ID: ALA4451018

Chembl Id: CHEMBL4451018

PubChem CID: 155522120

Max Phase: Preclinical

Molecular Formula: C8H14N4O3

Molecular Weight: 214.22

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CCCn1nc(O)c(CC(N)C(=O)O)n1

Standard InChI:  InChI=1S/C8H14N4O3/c1-2-3-12-10-6(7(13)11-12)4-5(9)8(14)15/h5H,2-4,9H2,1H3,(H,11,13)(H,14,15)

Standard InChI Key:  FGCRXYQHIDORDD-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA4451018

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Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 214.22

Molecular Weight (Monoisotopic): 214.1066

AlogP: -0.65

#Rotatable Bonds: 5

Polar Surface Area: 114.26

Molecular Species: ZWITTERION

HBA: 6

HBD: 3

#RO5 Violations: ┄

HBA (Lipinski): 7

HBD (Lipinski): 4

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 1.41

CX Basic pKa: 8.80

CX LogP: -2.04

CX LogD: -3.83

Aromatic Rings: 1

Heavy Atoms: 15

QED Weighted: 0.60

Np Likeness Score: -0.25

References

1. Sainas S, Temperini P, Farnsworth JC, Yi F, Møllerud S, Jensen AA, Nielsen B, Passoni A, Kastrup JS, Hansen KB, Boschi D, Pickering DS, Clausen RP, Lolli ML..  (2019)  Use of the 4-Hydroxytriazole Moiety as a Bioisosteric Tool in the Development of Ionotropic Glutamate Receptor Ligands.,  62  (9): [PMID:30943028] [10.1021/acs.jmedchem.8b01986]

Source

Source(1):

• Scientific Literature